Distinguishing immunoglobulin G4-related disease from its pancreatobiliary mimics: Are we there now?

Abstract

Immunoglobulin G subclass 4 (IgG4)-related disease is a fibroinflammatory disorder characterized histopathologically by tumefactive lesions with storiform fibrosis and an IgG4-positive, plasma cellenriched lymphocytic infiltrate. It was initially described in the late twentieth century as a sclerosing type of autoimmune pancreatitis. In 2003… (More)
DOI: 10.1002/hep.28624

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